NM_001018113.3(FANCB):c.69T>C (p.Leu23=) AND not provided

Germline classification:: Likely benign (2 submissions)
Last evaluated:: Sep 1, 2018
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV000762608.26

Allele description [Variation Report for NM_001018113.3(FANCB):c.69T>C (p.Leu23=)]

NM_001018113.3(FANCB):c.69T>C (p.Leu23=)

Gene:

FANCB:FA complementation group B [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xp22.2

Genomic location:

Preferred name:

NM_001018113.3(FANCB):c.69T>C (p.Leu23=)

HGVS:

NC_000023.11:g.14865442A>G
NG_007310.1:g.12621T>C
NM_001018113.3:c.69T>CMANE SELECT
NM_001324162.2:c.69T>C
NM_152633.4:c.69T>C
NP_001018123.1:p.Leu23=
NP_001311091.1:p.Leu23=
NP_689846.1:p.Leu23=
LRG_496t1:c.69T>C
LRG_496:g.12621T>C
NC_000023.10:g.14883564A>G
NM_001018113.1:c.69T>C
NR_136707.2:n.344T>C

Links:

dbSNP: rs151173533

NCBI 1000 Genomes Browser:

rs151173533

Molecular consequence:

NR_136707.2:n.344T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
NM_001018113.3:c.69T>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_001324162.2:c.69T>C - synonymous variant - [Sequence Ontology: SO:0001819]
NM_152633.4:c.69T>C - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000892941	CeGaT Center for Human Genetics Tuebingen	criteria provided, single submitter (CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)	Likely benign (Sep 1, 2018)	germline	clinical testing	Citation Link,
SCV005207996	Breakthrough Genomics, Breakthrough Genomics	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely benign	germline	not provided	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000892941

CeGaT Center for Human Genetics Tuebingen

criteria provided, single submitter

(CeGaT Center For Human Genetics Tuebingen Variant Classification Criteria Version 2)

Likely benign
(Sep 1, 2018)

germline

clinical testing

Citation Link,

SCV005207996

Breakthrough Genomics, Breakthrough Genomics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely benign

germline

not provided

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	yes	1	not provided	not provided	not provided	not provided	clinical testing, not provided

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From CeGaT Center for Human Genetics Tuebingen, SCV000892941.28

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	1	not provided	not provided	clinical testing	not provided

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		1	not provided	not provided	not provided

From Breakthrough Genomics, Breakthrough Genomics, SCV005207996.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	not provided	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Oct 20, 2024

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